Label: PHYTOPLEX CLEAR AID- white petrolatum,zinc oxide paste
- NDC Code(s): 53329-136-10
- Packager: Medline Industries, LP
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 29, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
7-dehydrocholesterol, Aphanizomemnon flos-aquae (algae) extract, camellia sinenis (green tea) leaf extract, caprylic/capric triglycerides, corn starch, dimethicone, eugenia caryophyllus (clove) flower extract, glycerin, guar gum,
hydrolyzed soy protein, manuka honey, phospholipids, tocopheryl acetate, water, yeast ferment extract, zea mays (corn) oil.
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Manufacturing Information
Phytoplex, Medline Remedy and Medline are registered trademarks of and Clear Aid is a trademark of Medline Industries, Inc.
Manufactured for Medline Industries, LP
Three Lakes Drive, Northfield, IL 60093 USA
Made in USA of domestic and imported materials
www.medline.com
1-800-MEDLINE
REF: MSC092502
RA19ULI
- Package Label
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INGREDIENTS AND APPEARANCE
PHYTOPLEX CLEAR AID
white petrolatum,zinc oxide pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53329-136 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 71.5 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 1 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6) WATER (UNII: 059QF0KO0R) YEAST (UNII: 3NY3SM6B8U) HONEY (UNII: Y9H1V576FH) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CLOVE (UNII: K48IKT5321) GUAR GUM (UNII: E89I1637KE) CORN OIL (UNII: 8470G57WFM) GREEN TEA LEAF (UNII: W2ZU1RY8B0) DIMETHICONE 20 (UNII: H8YMB5QY0D) STARCH, CORN (UNII: O8232NY3SJ) APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53329-136-10 71 g in 1 TUBE; Type 0: Not a Combination Product 07/01/2017 11/30/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 07/01/2017 11/30/2025 Labeler - Medline Industries, LP (025460908) Registrant - Medline Industries, LP (025460908)